The spectrum of paroxysmal dyskinesias
Paroxysmal dyskinesias (PxD) comprise a group of heterogeneous syndromes characterized by recurrent attacks of mainly dystonia and/or chorea, without loss of consciousness. PxD have been classified according to their triggers and duration as paroxysmal kinesigenic dyskinesia, paroxysmal nonkinesigen...
Saved in:
Published in | Future neurology Vol. 14; no. 3 |
---|---|
Main Author | |
Format | Journal Article |
Language | English |
Published |
London
Future Medicine Ltd
01.08.2019
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Paroxysmal dyskinesias (PxD) comprise a group of heterogeneous syndromes characterized by recurrent attacks of mainly dystonia and/or chorea, without loss of consciousness. PxD have been classified according to their triggers and duration as paroxysmal kinesigenic dyskinesia, paroxysmal nonkinesigenic dyskinesia and paroxysmal exertion-induced dyskinesia. Of note, the spectrum of genetic and nongenetic conditions underlying PxD is continuously increasing, but not always a phenotype–etiology correlation exists. This creates a challenge in the diagnostic work-up, increased by the fact that most of these episodes are unwitnessed. Furthermore, other paroxysmal disorders, included those of psychogenic origin, should be considered in the differential diagnosis. In this review, some key points for the diagnosis are provided, as well as the appropriate treatment and future approaches discussed. |
---|---|
ISSN: | 1479-6708 1748-6971 |
DOI: | 10.2217/fnl-2018-0047 |